Iridium Complexes in Organic Synthesis

Iridium Complexes in Organic Synthesis
Author: Luis A. Oro
Publisher: John Wiley & Sons
Total Pages: 424
Release: 2008-12-03
Genre: Science
ISBN: 3527623086

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Ranging from hydrogenation to hydroamination, cycloadditions and nanoparticles, this first handbook to comprehensively cover the topic of iridium in synthesis discusses the important advances in iridium-catalyzed reactions, namely the use of iridium complexes in enantioselective catalysis. A must for organic, complex and catalytic chemists, as well as those working with/on organometallics.

Synthesis and Characterization of Some Novel Iridium-, Iron-, and Cobalt-monocarborane Complexes

Synthesis and Characterization of Some Novel Iridium-, Iron-, and Cobalt-monocarborane Complexes
Author: Robin A. McCown
Publisher:
Total Pages:
Release: 2010
Genre:
ISBN:

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Reaction of the fragments {Ir(PEt3)n}+ with the monocarborane anion [closo-1-CB7H8]- causes an oxidative insertion to occur, and the iridium moiety to become a cluster vertex. This reaction provides two distinct, neutral, 9-vertex {IrCB7} products, depending on the ratio of iridium and phosphine reactants used. The iridium centers in these products have differing oxidation states, illustrating the exceptional ability of the smaller anionic monocarborane ligands to stabilize metals in higher oxidation states. Although salts of the 11-vertex anionic species [1,1,1-(CO)3-closo-1,2-FeCB9H10]- have resisted synthesis in the past, its analogue [1,1,1-(CO)3-2-Ph-closo-1,2-FeCB9H9]- has now been prepared. Moreover, two reactions demonstrating the derivative chemistry of this compound have been discovered. Previously, 10- and 12-vertex dicobalt monocarboranes were prepared and studied by treating monocarboranes with [Co2(CO)8]. This produced several poly-cobalt anions. New derivatives of these anions have been synthesized, using protocols developed since their discovery.

Synthesis, Characterization and Reactivity of Ylidyne and μ-Ylido Complexes Supported by Scorpionato Ligands

Synthesis, Characterization and Reactivity of Ylidyne and μ-Ylido Complexes Supported by Scorpionato Ligands
Author: Priyabrata Ghana
Publisher: Springer
Total Pages: 345
Release: 2019-01-01
Genre: Science
ISBN: 9783030026240

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This book explores the development of the first open-shell heavier tetrylidyne complexes featuring a tetrel-centered unpaired electron, and unprecedented metallatetrylidynes containing a multiply-bonded, linear-coordinated single heavier tetrel atom embedded between two metal centers. The chemistry of compounds featuring triple bonds of the heavier Group-14 elements Si–Pb with transition metals is a very challenging research area, which combines modern molecular main-group element with transition-metal chemistry, and is of fundamental importance for the understanding of chemical bonding. During the last 15 years, the research in this area has witnessed considerable progress in isolating a series of closed-shell tetrylidyne complexes. However, despite numerous attempts, open-shell tetrylidyne complexes and heavier group 14 element congeners of metallacarbynes and carbide complexes remained inaccessible. In this book, readers will find more about the reactivity studies of these novel complexes that uncovered a plethora of exceptional products, including a novel m3-silicido complex, the first dimetallasilacumulene with a linear, two-coordinated single silicon atom and the first compounds of planar tetracoordinated silicon (ptSi) (Anti-van’t Hoff-Le Bell Silicon). Readers will also learn about the isolation and full characterization of the first room-temperature stable disilavinylidene, a silicon analogue of the very reactive vinylidenes (R2C=C:), and the first intermetallic plumbylidyne ligand transfer reactions.